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100 mm macro lens

Manufactured by Canon
Sourced in Japan

The 100 mm macro lens is a professional-grade optical lens designed for high-quality close-up photography. It features a focal length of 100 mm and a maximum aperture of f/2.8, enabling precise focus and control over depth of field. The lens is constructed with high-quality materials and optical elements to deliver sharp, detailed images.

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10 protocols using 100 mm macro lens

1

Standardized Dental Photography Protocol

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All observational and interview studies were performed in the Orthodontics Department of Istanbul University; the overall research methodology could be considered a contextual inquiry [12 ]. To ensure reliable results from all participants, the photography procedure was standardised as previously described [13 , 14 (link)]. All photographs were taken by the same professional technician who was in charge of this procedure for the department. A Canon EOS 60D digital single lens reflex (DSLR) camera with a 100-mm Macro Lens and a Canon MR-14EX Macro Ring-Lite (Canon, Tokyo, JP) was used for photography (Figure 1).
The process of dental photography was investigated in three stages: portrait and profile photographs; intraoral frontal and profile photographs; and intraoral buccal and occlusal photographs. A plain, coloured background was used in stage 1; spandex (Hager & Werken, Duisburg, DE) and wire type cheek retractors (Masel, Bristol, PA) were used in stage 2; and both retractors and dental mirrors (Ortho Technology, Florida, USA) were used in stage 3 (Figure 2). A bowl of hot water was used to warm the mirrors to avoid fogging, which is a commonly used method among clinicians. All of these items are likely to influence the patient experience at certain points during the procedure.
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2

Measuring Water Contact Angle on PDMS

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The contact angle between the water droplet and the PDMS surface was measured by placing a 10 µL droplet of deionised water on the surface of PDMS slabs (Sylgard® 184, Dowsil, cured at 120 °C for 20 min) using a pipette (Eppendorf). Contact angle images were taken using a Canon 6D camera coupled with a Canon 100 mm macro lens. The contact angles were then measured using ImageJ.
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3

Blood Cell Velocity Measurement

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A Canon Rebel T3i camera and Canon 100 mm macro lens mounted on a copy stand were used to obtain images of the entire animal. Higher magnifications, required to follow moving blood cells, was obtained using a Meiji stereoscopic microscope and the Canon camera. Images were processed using Adobe Photoshop software with any image enhancement applied uniformly to the entire frame. The velocity of blood cells was determined by measuring position of a selected cell in sequential frames from a video. Video files were converted to individual images using QuickTime Player 7 (Apple) and the positions of cells were determined using Photoshop (Adobe). The default configuration of Photoshop gives x,y positions to 0.1 pixel, which is useful when one wants to specify the center of an object of 3–16 pixels. There are many other combinations of applications that could obtain similar data. In this report velocity is defined as distance/time, where time is 1/30 s, the time between each video frame, and data in graphs representing a moving average over 5 time points.
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4

Standardized Digital Imaging of Dental Enamel

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A digital camera (EOS 100D; Canon, Tokyo, Japan) with a 100-mm macro lens (Canon) was used to obtain DIs of the enamel blocks. All samples were photographed in a dark room under a manual camera setting (aperture, f5.6; shutter speed, 1/125s; ISO sensitivity, 400). The photographic procedure was standardized by mounting the camera on a rigid copystand at a distance of 38 cm from the enamel surface. The light source consisted of two lamps set at a 45° angle to the axis of the lens. All photographs were obtained at T1, T2, and T3.
The CIE L*a*b* values were acquired for sound enamel (P1) and WSL areas (P2) using Photoshop (Adobe Systems, San Jose, CA, USA; Figure 1B), which enabled the direct comparison of color differences between P1 and P2. P1 and P2 were positioned 1.5 mm from the incisal and gingival margins of the enamel blocks and mesiodistally centered. The color difference (ΔE*DI) between P1 and P2 was calculated as follows: ΔE*DI = [(L*P1 − L*P2)2 + (a*P1 − a*P2)2 + (b*P1 − b*P2)2]1/2.
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5

Dental Bracket Placement Accuracy Analysis

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Errors in bracket placement were compared between the two groups using dental models and individual pictures of each tooth.

Images were captured with a Canon digital camera and 100 mm macro lens set at 1:1 magnification and ring light.

To ensure consistency, a jig was built using a rectangle wire (1925 inches) spaced at 150 millimeters.

All further measurements are obtained by use imageJ.

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6

Behavior and Imagery of Notodontid Moth Species

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Theroa zethus and Praeschausia zapata behaviors were recorded in the lab on potted euphorbs with intact latex canals using a Wild M400 photomacroscope outfitted with a Canon T3i or T4i camera. Photographs of Datana perspicua and P. zapata in the field were taken using the same cameras with a Canon 100 mm macro lens. Other notodontid species were photographed and filmed in the lab on detached oak branches; the Canon cameras, 100 mm macro lens or Canon MP-E 65 mm lens, and various light sources including ring lights and LED light panels were used.
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7

Measuring Male Insect Morphology

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Males and females were separated by examining each specimen for the presence of an aedeagus. Using a jig, each pinned male specimen was then visually aligned to a standardized position and orientation in order to make lateral photographic images (Canon 500D camera body fitted with a Canon 100 mm macro lens set to manual focus) from which measurements were made (Fig. 1). Because the head, pronotum and elytra move in relation to one another, two images were made for each specimen, one for measuring elytral length and one for measuring horn length in side view. For measuring elytron length, the specimen was viewed from the side and tilted slightly until the elytral suture became entirely visible when the camera was triggered and the photograph stored for measurement. A measurement was then made from the anterior end of the left elytron along the margin to the posterior end. For measuring horn length, the specimen was tilted until the maximum visible horn area was seen and the second photograph was stored. The measurement was made from where the horn starts rising off the clypeus to the furthest tip of the horn. Each image had a gauge of known length to scale the images. Measurements were made using the program Analyzing Digital Images by John Pickle (Concord Academy; formerly, Museum of Science, Boston). Terminology for the male genitalia follows Medina et al. (2013) .
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8

Quantifying Cement Penetration in Knee Arthroplasty

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To analyze the cement penetration, digital photographs (72 dpi) were made of each cross-section using a Canon EOS 30D camera and a 100-mm macrolens on a tripod on a standardized setup (►Fig. 4) . A measuring staff to correct for any magnification error accompanied every cross-section. Adobe Photoshop (version 13.0.1) was used to analyze the images.
To exclude the irregularities around the tibial fin, two standardized areas (one anterior and one posterior of the fin) of 600 Â 600 pixels (averaging 1.5 Â 1.5 cm) were measured. Using the "Magic Wand tool," the area with cement was selected and measured (►Fig. 5). To acquire the average penetration depth, the measured total area was divided by the total length. If there were areas without cement, the separate areas were measured and added to achieve the total area and length.
The femur was analyzed in a similar manor, again using the "Magic Wand tool." We made a distinction between the ante-rior, distal (including anterior and posterior chamfer cuts), and posterior surfaces (►Fig. 6). The distal, anterior, and posterior surfaces were again analyzed for average cement penetration, as described by the method earlier. Due to the fact that in both techniques the cement was applied on the posterior condyles of the femoral implant, we did not compare these results.
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9

Characterization of Dry Tropical Forest Lichens

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The material deposited in the herbaria TULV (INCIVA) and CUVC at Universidad del Valle, Colombia, collected in the framework of the project aimed at contributing to the conservation of Valle del Cauca dry tropical forests (OCAD n° 61 del 7/11/2017 bpin_2016000100013 de 7 de noviembre 2017), was examined. The samples were examined to determine the characteristics of the thallus and ascomata, as well as their reaction to UV light and the type and size of the ascospores, using a stereoscope (YAXUN YXAK21) and a microscope (CARL ZEISS Jena) while ascospores were measured with a micrometer ruler. All samples were photographed with a VIVITAR 100 mm macro lens adjusted to a CANON T3 digital camera. Van den Broeck, et al. (2018) was used to key out the species.
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10

Specimen Documentation Protocol

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In this study we examined specimens and photographs of specimens housed in the following depositories: The order which the descriptions follow is the same as the species key out in the key below.
Locality labels are reported verbatim with author comments in square brackets.
Color photographs were obtained using a Canon 500D body with either a Canon 100mm macro lens or Canon 65mm MPE 1-5x zoom lens. Image stacking was done using Helicon remote and Helicon focus software.
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